Variant to disease dataset workflows for Open Targets Genetics
☆14May 11, 2026Updated last month
Alternatives and similar repositories for genetics-v2d-data
Users that are interested in genetics-v2d-data are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆10Dec 29, 2021Updated 4 years ago
- This is a virtual environment which contains databases, software, workflows, and workshops for Precision Health Data Analysis.☆23Mar 31, 2023Updated 3 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- Automated CWL and Galaxy XML generation for Python tools that use argparse and click☆11Jul 29, 2019Updated 6 years ago
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Aug 17, 2021Updated 4 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Program for estimating admixture proportions and doing principal component analysis of a single NGS sample☆12Aug 15, 2024Updated last year
- Ontology for Immune Epitopes☆13Updated this week
- A high-throughput analysis framework for Y-chromosomal next-generation sequencing data☆17Jun 11, 2021Updated 5 years ago
- A web tool that helps biomedical researchers understand how their work is being used by others, by analyzing the content in papers that c…☆13Oct 19, 2018Updated 7 years ago
- CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data☆12Nov 9, 2025Updated 7 months ago
- 🐶 hlabud: HLA genotype analysis in R☆19Apr 11, 2025Updated last year
- Geneyx Analysis API☆12Jun 10, 2026Updated 2 weeks ago
- Heritability, genetic correlation and functional enrichment estimation for case-control studies☆20Nov 26, 2023Updated 2 years ago
- Training scripts for BERTax☆12Jun 12, 2024Updated 2 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Reads the output from CLI help commands, and generates machine readable schemas (CWL etc)☆14Feb 14, 2021Updated 5 years ago
- Scripts for reading, extracting, and organizing data from either HTML or PDF documents and prepare them to be converted into embeddings f…☆13Aug 26, 2024Updated last year
- [DEPRECATED] Docker containers for Bioconductor☆49Mar 15, 2023Updated 3 years ago
- Analysis and figure generation code for the ABRF NGS Phase II Study on DNA-seq reproducibility☆18Aug 5, 2021Updated 4 years ago
- ☆11Oct 2, 2024Updated last year
- iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Genera…☆16Jun 11, 2026Updated 2 weeks ago
- JanusDNA☆31Mar 19, 2026Updated 3 months ago
- Estimate similarity of medical concepts based on Unified Medical Language System (UMLS)☆16Jan 17, 2022Updated 4 years ago
- hail-based pipelines for annotating variant callsets and exporting them to clickhouse☆23Updated this week
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- Specification for the GWAS-VCF format (manuscript in preparation)☆26Aug 3, 2021Updated 4 years ago
- ☆11Jan 30, 2025Updated last year
- A Silver Standard Corpus of Human Phenotype-Gene Relations☆13Oct 6, 2022Updated 3 years ago
- Automatic classification of sequence variants and CNVs according to ACMG criteria.☆31Sep 30, 2024Updated last year
- Pynocular is a lightweight ORM that lets you query your database using Pydantic models and asyncio☆11May 24, 2022Updated 4 years ago
- Welcome page and service overview☆18Mar 29, 2023Updated 3 years ago
- Code to reproduce analysis and figures for 'Genetic mapping of etiologic brain cell types for obesity' (Timshel, eLife 2020)☆14May 20, 2021Updated 5 years ago
- A Python package for creating high-quality manhattan and Q-Q plots from GWAS results.☆52Dec 27, 2023Updated 2 years ago
- Course material for "Dynamically adding and removing Shiny modules"☆26Aug 15, 2022Updated 3 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- CWL for GDC DNASeq workflows☆24Mar 30, 2026Updated 2 months ago
- R as a backend for web apps.☆10Mar 7, 2018Updated 8 years ago
- 🌓 Allele specific analyses across cell states and conditions☆10Nov 28, 2022Updated 3 years ago
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 7 years ago
- Training material for the GWAS Catalog REST API workshop☆13May 22, 2023Updated 3 years ago
- Workflow Execution Service Backend☆21Jun 22, 2026Updated last week
- Jupyter Notebooks and other code for 4CE data visualizations.☆13Jan 25, 2023Updated 3 years ago